NDC 49288-0295

Mucor Mixture

Mucor Mixture is a Intradermal; Subcutaneous Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Antigen Laboratories, Inc.. The primary component is Mucor Plumbeus; Mucor Racemosus; Rhizopus Stolonifer.

Product ID	49288-0295_272c9910-2160-4d41-afbd-faab3055ba1d
NDC	49288-0295
Product Type	Human Prescription Drug
Proprietary Name	Mucor Mixture
Generic Name	Mucor Mixture
Dosage Form	Injection, Solution
Route of Administration	INTRADERMAL; SUBCUTANEOUS
Marketing Start Date	1974-03-23
Marketing Category	BLA / BLA
Application Number	BLA102223
Labeler Name	Antigen Laboratories, Inc.
Substance Name	MUCOR PLUMBEUS; MUCOR RACEMOSUS; RHIZOPUS STOLONIFER
Active Ingredient Strength	0 g/mL; g/mL; g/mL
Pharm Classes	Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [CS],Allergens [CS],Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [CS],Allergens [CS],Non-Standardized Fungal Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Increased IgG Production [PE],Fungal Proteins [CS],Allergens [CS]
NDC Exclude Flag	E
Listing Certified Through	2017-12-31

Packaging

NDC 49288-0295-1

2 mL in 1 VIAL, MULTI-DOSE (49288-0295-1)

Marketing Start Date	1974-03-23
NDC Exclude Flag	N
Sample Package?	N

NDC SPL Data Element Entries

NDC 49288-0295-5 [49288029505]

Mucor Mixture INJECTION, SOLUTION

Marketing Category	BLA
Application Number	BLA102223
Product Type	HUMAN PRESCRIPTION DRUG
Marketing Start Date	1974-03-23
Inactivation Date	2019-10-21

NDC 49288-0295-1 [49288029501]

Mucor Mixture INJECTION, SOLUTION

Marketing Category	BLA
Application Number	BLA102223
Product Type	HUMAN PRESCRIPTION DRUG
Marketing Start Date	1974-03-23
Inactivation Date	2019-10-21

NDC 49288-0295-4 [49288029504]

Mucor Mixture INJECTION, SOLUTION

Marketing Category	BLA
Application Number	BLA102223
Product Type	HUMAN PRESCRIPTION DRUG
Marketing Start Date	1974-03-23
Inactivation Date	2019-10-21

NDC 49288-0295-2 [49288029502]

Mucor Mixture INJECTION, SOLUTION

Marketing Category	BLA
Application Number	BLA102223
Product Type	HUMAN PRESCRIPTION DRUG
Marketing Start Date	1974-03-23
Inactivation Date	2019-10-21

NDC 49288-0295-3 [49288029503]

Mucor Mixture INJECTION, SOLUTION

Marketing Category	BLA
Application Number	BLA102223
Product Type	HUMAN PRESCRIPTION DRUG
Marketing Start Date	1974-03-23
Inactivation Date	2019-10-21

Drug Details

Active Ingredients

Ingredient	Strength
MUCOR PLUMBEUS	.0167 g/mL

OpenFDA Data

SPL SET ID:	6d2006e2-55ea-41db-bd17-ce6d080f28a0
Manufacturer	Antigen Laboratories, Inc.
UNII	91M9RWP3TD 3F36V0451W 199I7J3JIV 6JR6JTN25S 2072U60DUI D1A2NG69CK W5U19AK212 41Y752Y34M 1X92VM01YP HR6H5057CO Y0M7LGE3Z8 GQM6LVU5V8 KO7V58BY40 3Y1PE1GCIG TGO054E31O 4K7Z7K7SWG T8678F0P0Q 6K41G30A6U 2ZAU32517N A17SE577FM DHI513VXU7 0N3Z1P4B2W 2VWV12V9WR T069R9OPVG TBW53313S7 HJ4L70T1ZP BV82OL2IZ8 17RH99LQ7G 52B29REC7H B7B86Y84R8 KSY1AWN59I 7ORP6R724L 1XSC3BB35Z H20KU95UBG 87U156LEN7 AZJ5XKM7W3 1M4E76V32I 9IOA40ANG6 5398RXP8KU FEE198DK4Q 5016WB8B8A X92O101CS2 RZ55S3AQOJ 5964J742O8 978D8U419H 9Y53ZS6I82 3J888Y9L13 O64JF11198 49VI1ZSO06 N4F4RQ7BY7 VK8C112WTS 15W81V867R SQ89E6LOME X88DF51T48 C91ZMT66YA G0O5980Z7W 3LN5B70U4W YIH315U1TU 4ZWY20GTGO Z4MD1809H1 Q222J2186W 4D7G21HDBC 0V3J4YEX2W D7401PWY6E
RxNorm Concept Unique ID - RxCUI	1232665 1232664 854133 1006282 852401 1232661 1006288 852243 905075 314941 968126 995702 968128 889590 852394 1011972 1014388 1012051 1012035 852131 892348 1192733 967724 883483 883481 892341 905073 852060 883409 968440 966660 1006300 852105 966984 966982 1014440 1192974 1192972 1006313 968495 1014754 901848 966993 967051 966998 852192 1192996 968544 967985 968429 967038 968425 967036 968420 967030 1014748 852041 852690 967777 905091 967049 968416 967963 967000 967967 967969 852375 968406 968404 1192735 1193007 1193001 1094477 967761 968814 967053 995697 852469 1014761 966946 966695 968470 967061 1193013 968478 1010904 968509 967947 904834 967371 1014402 968505 1014410 995730 967032 1014390 1014394 1012047 1014398 968117
Pharm Class PE	Cell-mediated Immunity [PE] Increased IgG Production [PE] Increased Histamine Release [PE]
PHarm Class EPC	Non-Standardized Fungal Allergenic Extract [EPC]
NUI Code	N0000185001 N0000175629 N0000171131 N0000185372 N0000169106 N0000184306

Pharmacological Class

Non-Standardized Fungal Allergenic Extract [EPC]
Increased Histamine Release [PE]
Cell-mediated Immunity [PE]
Increased IgG Production [PE]
Fungal Proteins [CS]
Allergens [CS]
Non-Standardized Fungal Allergenic Extract [EPC]
Increased Histamine Release [PE]
Cell-mediated Immunity [PE]
Increased IgG Production [PE]
Fungal Proteins [CS]
Allergens [CS]
Non-Standardized Fungal Allergenic Extract [EPC]
Increased Histamine Release [PE]
Cell-mediated Immunity [PE]
Increased IgG Production [PE]
Fungal Proteins [CS]
Allergens [CS]

NDC Crossover Matching brand name "Mucor Mixture" or generic name "Mucor Mixture"

NDC	Brand Name	Generic Name
49288-0294	Mucor Mixture	Mucor Mixture
49288-0295	Mucor Mixture	Mucor Mixture